NDC 67777-412 Dynarex Burn Cream
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 67777 - Dynarex Corporation
- 67777-412 - Dynarex Burn Cream
Product Packages
NDC Code 67777-412-01
Package Description: .9 g in 1 PACKET
Product Details
What is NDC 67777-412?
What are the uses for Dynarex Burn Cream?
Which are Dynarex Burn Cream UNII Codes?
The UNII codes for the active ingredients in this product are:
- LIDOCAINE HYDROCHLORIDE (UNII: V13007Z41A)
- LIDOCAINE (UNII: 98PI200987) (Active Moiety)
- BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7)
- BENZALKONIUM (UNII: 7N6JUD5X6Y) (Active Moiety)
Which are Dynarex Burn Cream Inactive Ingredients UNII Codes?
The inactive ingredients are all the component of a medicinal product OTHER than the active ingredient(s). The acronym "UNII" stands for “Unique Ingredient Identifier” and is used to identify each inactive ingredient present in a product. The UNII codes for the inactive ingredients in this product are:
- ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS)
- METHYLCELLULOSE (25 MPA.S) (UNII: BI55GG2WLI)
- CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)
- GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)
- DIMETHICONE (UNII: 92RU3N3Y1O)
- CETETH-20 (UNII: I835H2IHHX)
- BUTYLATED HYDROXYTOLUENE (UNII: 1P9D0Z171K)
- METHYLPARABEN SODIUM (UNII: CR6K9C2NHK)
- PROPYLPARABEN SODIUM (UNII: 625NNB0G9N)
- GLYCERIN (UNII: PDC6A3C0OX)
- EDETATE SODIUM (UNII: MP1J8420LU)
- WATER (UNII: 059QF0KO0R)
What is the NDC to RxNorm Crosswalk for Dynarex Burn Cream?
- RxCUI: 1012100 - benzalkonium chloride 0.13 % / lidocaine HCl 0.5 % Topical Cream
- RxCUI: 1012100 - benzalkonium chloride 1.3 MG/ML / lidocaine hydrochloride 5 MG/ML Topical Cream
- RxCUI: 1012100 - benzalkonium chloride 0.13 % / lidocaine hydrochloride 0.5 % Topical Cream
* Please review the disclaimer below.
[5] What is the Labeler Name? - Name of Company corresponding to the labeler code segment of the Product NDC.
[9] What is the Start Marketing Date? - This is the date that the labeler indicates was the start of its marketing of the drug product.
[11] What is the Listing Expiration Date? - This is the date when the listing record will expire if not updated or certified by the product labeler.
[12] What is the NDC Exclude Flag? - This field indicates whether the product has been removed/excluded from the NDC Directory for failure to respond to FDA"s requests for correction to deficient or non-compliant submissions ("Y"), or because the listing certification is expired ("E"), or because the listing data was inactivated by FDA ("I"). Values = "Y", "N", "E", or "I".